Valproic

Product NDC

0615-7840

11-digit product format

006157840

Labeler code

0615

Product ID

0615-7840_0f5cd26d-1274-444a-bdfd-eb8f7476d1f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valproic Acid

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA073229

Marketing category

ANDA

Marketing start

2009-09-08

Marketing end

0000-00-00

Substance

VALPROIC ACID

Active strength

250 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record